JARIT SURGICAL INSTRUMENTS— 510(k) K932072

Name: FDA 510(k) clearance K932072
Creator: U.S. Food and Drug Administration
Published: 1994-01-11

Substantially Equivalent

Medical Device Inspection Co., Inc.

FDA 510(k) clearance K932072 for JARIT SURGICAL INSTRUMENTS, Substantially Equivalent on 1994-01-11. Applicant: Medical Device Inspection Co., Inc.. Device class: 2.

Clearance details

Applicant: Medical Device Inspection Co., Inc.
Product code: Code HET
Device class: Class 2
Regulation: 21 CFR 884.1720
Advisory panel: Obstetrics/Gynecology
Date received: 1993-04-28
Decision date: 1994-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HET

view all

K250939 — SIRIUS Endoscope System (PR-SI-1230)2025-08-29
K243821 — i-Cut2025-04-25
K221642 — SIRIUS Endoscope System2022-12-12
K210116 — Video Endoscopy System, 3D Video Endoscopy System2021-10-13
K201832 — Endoeye Flex Deflectable Videoscope Olympus LTF-S190-52021-09-17

More clearances from Medical Device Inspection Co., Inc.

view all

K945826 — J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS1995-08-04
K931594 — THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM1993-12-21
K933578 — POWERMATIC MAT PLATFORM1993-11-05
K933580 — POWER WORK TABLE1993-11-05
K933581 — POWERMATIC TREATMENT TABLE1993-11-05

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.